Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_assertion description "[Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_assertion evidence source_evidence_literature NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_assertion SIO_000772 19855393 NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_assertion wasDerivedFrom befree-2016 NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_assertion wasGeneratedBy ECO_0000203 NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.
- befree-2016 importedOn "2016-02-19" NP771578.RAU5WnQDj2Rdn38-v1KwY5fnYrfjR1BIXCUimBkIYT-sw130_provenance.